Clinical experience of laboratory follow‐up with noninvasive prenatal testing using cell‐free DNA and positive microdeletion results in 349 cases von Schwartz, S., Kohan, M., Pasion, R., Papenhausen, P. R., Platt, L. D.

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Subtelomere FISH analysis of 11 688 cases: an evaluation of the frequency and pattern of subtelomere rearrangements in individuals with developmental disabilities von Ravnan, J B, Tepperberg, J H, Papenhausen, P, Lamb, A N, Hedrick, J, Eash, D, Ledbetter, D H, Martin, C L

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Interstitial Deletion of Proximal 8q Including Part of the Centromere from Unbalanced Segregation of a Paternal Deletion/Marker Karyotype with Neocentromere Formation at 8p22 von Burnside, R.D., Ibrahim, J., Flora, C., Schwartz, S., Tepperberg, J.H., Papenhausen, P.R., Warburton, P.E.

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Epigenetic detection of human chromosome 14 uniparental disomy von Murphy, S.K., Wylie, A.A., Coveler, K.J., Cotter, P.D., Papenhausen, P.R., Sutton, V.R., Shaffer, L.G., Jirtle, R.L.

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Prenatal molecular cytogenetic diagnosis of partial tetrasomy 10p due to neocentromere formation in an inversion duplication analphoid marker chromosome von Levy, B., Papenhausen, P.R., Tepperberg, J.H., Dunn, T.M., Fallet, S., Magid, M.S., Kardon, N.B., Hirschhorn, K., Warburton, P.E.

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Refined molecular characterization of the breakpoints in small inv dup(15) chromosomes von HUANG, B, CROLLA, J. A, CHRISTIAN, S. L, WOLF-LEDBETTER, M. E, MACHA, M. E, PAPENHAUSEN, P. N, LEDBETTER, D. H

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Phenotypes Associated with SHOX Deficiency von Ross, Judith L., Scott, Charles, Marttila, Pia, Kowal, Karen, Nass, Andrea, Papenhausen, Peter, Abboudi, Jack, Osterman, Lee, Kushner, Harvey, Carter, Peter, Ezaki, Marybeth, Elder, Frederick, Wei, Fanglin, Chen, Huaqun, Zinn, Andrew R.

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Phenotypes Associated with SHOX Deficiency von Ross, J L, Scott, Jr, C, Marttila, P, Kowal, K, Nass, A, Papenhausen, P, Abboudi, J, Osterman, L, Kushner, H, Carter, P, Ezaki, M, Elder, F, Wei, F, Chen, H, Zinn, A R

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Xp pseudoautosomal gene haploinsufficiency and linear growth deficiency in three girls with chromosome Xp22;Yq11 translocation von Joseph, M, Cantú, E S, Pai, G S, Willi, S M, Papenhausen, P R, Weiss, L

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Tetrasomy 15q26: a distinct syndrome or Shprintzen-Goldberg syndrome phenocopy? von Levy, Brynn, Tegay, David, Papenhausen, Peter, Tepperberg, James, Nahum, Odelia, Tsuchida, Tammy, Pletcher, Beth A., Ala-Kokko, Leena, Baker, Stuart, Frederick, Barbara, Hirschhorn, Kurt, Warburton, Peter, Shanske, Alan

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Twin-twin transfusion syndrome in a dizygotic monochorionic-diamniotic twin pregnancy von Quintero, R A, Mueller, O T, Martínez, J M, Arroyo, J, Gilbert-Barness, E, Hilbelink, D, Papenhausen, P, Sutcliffe, M

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Lowe oculocerebrorenal syndrome in a female with a balanced X;20 translocation : mapping of the X chromosome breakpoint von MUELLER, O. T, HARTSFIELD, J. K, GALLARDO, L. A, ESSIG, Y.-P, MILLER, K. L, PAPENHAUSEN, P. R, TEDESCO, T. A

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Burkitt lymphoma arising in organ transplant recipients: A clinicopathologic study of five cases von GONG, Jerald Z, STENZEL, Timothy T, BENNETT, Ellen R, LAGOO, Anand S, DUNPHY, Cherie H, MOORE, Joseph O, RIZZIERI, David A, TEPPERBERG, James H, PAPENHAUSEN, Peter, BUCKLEY, Patrick J

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Case report of spontaneous remission of cytogenetic relapse of chronic myelogenous leukemia suggestive of progression to blast crisis after allogeneic bone marrow transplantation von AGALIOTIS, D. P, PANEHAUSEN, P. R, MOSCINSKI, L. C, ELFENBEIN, G. J

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Twin-twin transfusion syndrome in a dizygotic monochorionic-diamniotic twin pregnancy von Quintero, R. A., Mueller, O. T., Martínez, J. M., Arroyo, J., Gilbert-Barness, E., Hilbelink, D., Papenhausen, P., Sutcliffe, M.

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Spectral karyotyping refines cytogenetic diagnostics of constitutional chromosomal abnormalities von Schröck, E, Veldman, T, Padilla-Nash, H, Ning, Y, Spurbeck, J, Jalal, S, Shaffer, L G, Papenhausen, P, Kozma, C, Phelan, M C, Kjeldsen, E, Schonberg, S A, O'Brien, P, Biesecker, L, du Manoir, S, Ried, T

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Refined molecular characterization of the breakpoints in small inv dup(15) chromosomes von Huang, B., Crolla, J. A., Christian, S. L., Wolf-Ledbetter, M. E., Macha, M. E., Papenhausen, P. N., Ledbetter, D. H.

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Oncogene amplification in transforming myelodysplasia von Papenhausen, Peter R., Griffin, Sharon, Tepperberg, James

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Tissue limited mosaicism in a patient with tetrasomy 9p von Papenhausen, Peter, Riscile, Gisele, Miller, Karen, Kousseff, Boris, Tedesco, Thomas

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Spectral karyotyping refines cytogenetic diagnostics of constitutional chromosomal abnormalities von SCHRÖCK, E, VELDMAN, T, KJELDSEN, E, SCHONBERG, S. A, O'BRIEN, P, BIESECKER, L, DU MANOIR, S, RIED, T, PADILLA-NASH, H, NING, Y, SPURBECK, J, JALAL, S, SHAFFER, L. G, PAPENHAUSEN, P, KOZMA, C, PHELAN, M. C

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